PURCOL ANTIBACTERIAL WIPES LEMON SCENT- benzalkonium chloride cloth

Purcol Antibacterial Wipes Lemon Scent by

Drug Labeling and Warnings

Purcol Antibacterial Wipes Lemon Scent by is a Otc medication manufactured, distributed, or labeled by Purocol LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antimicrobial

Uses

• For hand washing to decrease bacteria on skin.
• Recommended for repeated use

Warnings

For external use only.

Do not use:

• in the eyes.
• if you are allergic to any of the ingredients.

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash appears and lasts for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away.

Directions

• Storage. Store at room temperature.
• Dispensing. Flip open the dispending cap. Peel back the security label. Remove wipes. To reseal: slightly press on dispensing cap.
• Use. Apply wipe thoroughly to hands or surfaces as desired. Allow to dry without wiping.
• Disposal. Dispose of used wipes in trash bin after use. Do not flush.

Inactive ingredients

Ethylhexylglycerin, Glycerin, Phenoxyethanol, Polyaminopropyl biguanide, Propylene Glycol, Purified water.

Package Labeling:

INGREDIENTS AND APPEARANCE

PURCOL ANTIBACTERIAL WIPES LEMON SCENT 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75266-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75266-001-01	80 in 1 POUCH	03/05/2021
1		2.5 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/05/2021

Labeler - Purocol LLC (117479056)

Establishment
Name	Address	ID/FEI	Business Operations
Purocol LLC		117479056	manufacture(75266-001) , label(75266-001) , pack(75266-001)